Canonical Allele Identifier: CA2942748
Gene: UGT2B15 HGNC NCBI

Linked Data

ClinVar Variation Id: 225966
dbSNP Id: rs1902023

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670366A>C , CM000666.2:g.68670366A>C GRCh38
NC_000004.11:g.69536084A>C , CM000666.1:g.69536084A>C GRCh37
NC_000004.10:g.69218679A>C NCBI36
NG_052676.1:g.5411T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000338206.6:c.253T>G MANE Select ENSP00000341045.5:p.Tyr85Asp
ENST00000338206.5:c.253T>G ENSP00000341045.5:p.Tyr85Asp
ENST00000616841.4:n.253T>G ENSP00000482004.1:p.Tyr85Asp
NM_001076.3:c.253T>G NP_001067.2:p.Tyr85Asp
NM_001076.4:c.253T>G MANE Select NP_001067.2:p.Tyr85Asp